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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 865347Generated: October 31, 2026

Potassium Permanganate → 5-(4-Cyanobenzyloxy)-2-nitrobenzoic acid

https://huagongshe.com/reaction/865347

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium PermanganateHCID 516875—
Reactant5-(4-Cyanobenzyloxy)-2-nitrobenzaldehydeHCID 22904973—
CatalystTetrabutylammonium BromideHCID 74236—
SolventPyridineHCID 1049—
Product5-(4-Cyanobenzyloxy)-2-nitrobenzoic acidHCID 22904955125.2%

Reaction Steps

Potassium permanganate (6.18 g, 39.1 mmol) was added in portions to a stirred solution of 13.8 g (48.9 mmol) of 5-(4-cyanobenzyloxy)-2-nitrobenzaldehyde and 1.58 g (4.89 mmol) of tetrabutylammonium bromide in 70 mL of pyridine. After 1 h, the solvent was removed in vacuo and the residue was partitioned between ethyl acetate and water. Sodium hydrogen sulfite was added to destroy excess permanganate and the aqueous phase was separated and extracted with ethyl acetate. The combined organics were washed with 1N sodium hydrogen sulfate, brine, dried over anhydrous magnesium sulfate, and concentrated to give 14.6 g of 5-(4-cyanobenzyloxy)-2-nitrobenzoic acid as a powder, used without further purification. 1H NMR (300 MHz, d6 -acetone) d 8.07 (1H, d, J=8.8 Hz, O-Ar-H), 7.86 (2H, d, J=8.3 Hz, NC-Ar-H2), 7.78 (2H, d, J=8.3 Hz, NC-Ar-H2), 7.39 (1H, d, J=2.9 Hz, O-Ar-H), 7.36 (1H, dd, J=8.8, 2.9 Hz, O-Ar-H), 5.48 (2H, s, ArCH2O).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05565449
Source datasetuspto-grants-1996_10
ORD IDord-99a8a2453a5244a5a7d012ced83e14ed
Source noteuspto-grants-1996_10